Interpretation and Optimization of the Dissolution Specifications for a Modified Release Product with an In Vivo–In Vitro Correlation (IVIVC)-Reference-Cited by-同舟云学术

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Interpretation and Optimization of the Dissolution Specifications for a Modified Release Product with an In Vivo–In Vitro Correlation (IVIVC)

Published:2004-03 Issue:3 Volume:93 Page:571-581
ISSN:0022-3549
Container-title:Journal of Pharmaceutical Sciences
language:en
Short-container-title:Journal of Pharmaceutical Sciences

Author:

Hayes Siobhán,Dunne Adrian,Smart Trevor,Davis John

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference31 articles.

1. Evaluation of U.S. pharmacopeia sampling plans for dissolution;Pheatt;J Qual Technol,1980

2. Dissolution testing of solid oral dosage forms,2002

3. Drug dissolution and bioavailability;Banakar,1994

4. Dissolution,1995

5. In vitro and in vivo evaluation of dosage forms,1995

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1. In silico, in situ, in vitro, and in vivo predictive methods for modeling formulation performance;From Current to Future Trends in Pharmaceutical Technology;2024

2. Application of the Simcyp Population‐based PBPK Simulator to the Modelling of MR Formulations;Oral Drug Delivery for Modified Release Formulations;2022-04-08

3. Pharmaceutical Product Lead Optimization for Better In vivo Bioequivalence Performance: A case study of Diclofenac Sodium Extended Release Matrix Tablets;Current Drug Delivery;2018-05-14

4. Development and Evaluation of Internal and External Predictability of Metoclopramide Hydrochloride Modified Release Formulations: An Establishment of Level A In vitro and In vivo Correlation;Indian Journal of Pharmaceutical Education and Research;2017-05-01

5. In Vitro/In Vivo Correlations;Developing Solid Oral Dosage Forms;2017

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